2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
98%
- Product Code: 209962
CAS:
882678-96-8
| Molecular Weight: | 233.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or vinyl halides under palladium catalysis. This makes it valuable in the development of complex organic molecules, especially in drug discovery and materials science. The presence of the amine group offers a handle for further functionalization, enabling multi-step syntheses where selective reactivity is required. It is particularly useful in creating substituted aromatic amines found in bioactive compounds and functional materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 250mg | 10-20 days | $11.19 |
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| 1g | 10-20 days | $43.24 |
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| 5g | 10-20 days | $337.21 |
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2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or vinyl halides under palladium catalysis. This makes it valuable in the development of complex organic molecules, especially in drug discovery and materials science. The presence of the amine group offers a handle for further functionalization, enabling multi-step syntheses where selective reactivity is required. It is particularly useful in creating substituted aromatic amines found in bioactive compounds and functional materials.
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